Effectiveness of the Combined WLI and Hyperthermia for GI Cancer Liver Metastasis
Primary Purpose
Hyperthermia
Status
Terminated
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Combined hyperthermia and radiation therapy
Sponsored by
About this trial
This is an interventional treatment trial for Hyperthermia
Eligibility Criteria
Inclusion Criteria:
- 1 Patients must have a diagnosis of pathologic proven gastrointestinal tract cancer
- 2 Unresectable and unsuitable to other local modalities
- 3 Not responded and/or unsuitable to chemotherapy
- 4 Eastern Cooperative Oncology Group ECOG) performance status 0 to 3
- 5 Assessment by colorectal tumor board (surgeon, radiation oncologist and medical oncologist participated)
- 6 Age ≥ 20
- 7 Agreement of study-specific informed consent
8 Blood work requirements
- Absolute neutrophil count (ANC) ≥ 1,500 /mm3, Platelet ≥ 50,000/mm3, Hgb ≥ 8 g/dl
- Liver function test(LFT): Total bilirubin<3.0 mg/dL, International normalized ratio(INR) < 1.7, Albumin ≥ 2.8g/dL, Aspartate aminotransferase (AST)/Alanine aminotransferase (ALT)< 6 X normal
- Serum creatinine < 1.5 X normal, or Creatinine clearance rate (CCr) ≥ 60 mL/min
- 9 Child-Pugh score 10 or less within 1 week before WLI
- 10 Childbearing potential woman, consent contraception at least 6 months
- 11 Stable breathing more than 5 minutes
Exclusion Criteria:
- 1 Life expectancy less than 8 weeks
- 2 Pregnant and/or breastfeeding woman
- 3 Previous upper abdominal RT history
- 4 Uncontrolled ascites or hepatic encephalopathy
- 5 Unstable respiration due to pleural effusion, chronic obstructive pulmonary disease COPD) etc
Sites / Locations
- Samsung Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Combined hypertermia and RT
Arm Description
Combined hypertermia and radiothearpy
Outcomes
Primary Outcome Measures
Time to Local Tumor Progression After Combined Hyperthermia and RT
Local progression will be defined as more than 20% size increase of metastatic lesions or new metastatic lesion in liver. Time to local tumor progression will be measured from the date of RT start to the date of local progression or last follow-up visit.
Secondary Outcome Measures
Objective Response Rate of Combined Hyperthermia and RT
Change in the Grade of Quality of Life at 3 Months From That Before the Combined Hyperthermia and RT
To measure the quality of life, European Organisation for Research and Treatment of Cancer (EORTC)- quality of life questionnaire (QLQ) 30 and Functional Assessment of Cancer Therapy-Hepatobiliary will be used. (grade 1 to 4, 1; not at all, 2; a little, 3; quite a bit, 4; very much)
Local Tumor Progression Free Survival Rate After Combined Hyperthermia and RT
Local progression will be defined as more than 20% size increase of metastatic lesions or new metastatic lesion in liver. Local progression free survival will be measured from the date of RT start to the date of local progression or last follow-up visit.
Adverse Event After Combined Hyperthermia and RT.
All grade III or higher toxicities (repeated measure)
Overall Survival Rate After Combined Hyperthermia and RT
Overall survival will be measured from the date of RT start to the date of death or last follow-up visit.
Full Information
NCT ID
NCT01963117
First Posted
September 25, 2013
Last Updated
March 18, 2020
Sponsor
Samsung Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01963117
Brief Title
Effectiveness of the Combined WLI and Hyperthermia for GI Cancer Liver Metastasis
Official Title
Effectiveness of the Combined Whole Liver Irradiation (WLI) and Hyperthermia for Unresectable Chemoresistant Multiple Liver Metastasis From Gastrointestinal Tract Cancer: Prospective Phase II Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2014
Overall Recruitment Status
Terminated
Why Stopped
Poor accrual
Study Start Date
October 2013 (undefined)
Primary Completion Date
November 2014 (Actual)
Study Completion Date
April 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Samsung Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The standard treatment of unresectable liver metastasis in gastrointestinal tract cancer is chemotherapy, but considerable portion of the patients progressed and most of the liver is converted to metastatic tumor lesions. Significant quality of life decrement was detected in those patients, especially in patients suffered severe symptoms Several studies reported that whole liver RT (WLRT) can be used effectively to control severe symptoms from unresectable liver metastasis in gastrointestinal tract cancer patients. However, it is well known fact that the liver is a very sensitive to RT. Despite symptom palliation is obtained after 20 to 30 Gy RT but only in small subset of patients get local control. In this aspect, the combined with radiosensitizer with WLRT is considered to enhance RT effect to palliate symptom and control local tumor progression, and increase the quality of life ultimately.
It is reported that hyperthermia is considered as the most valuable radiosensitizer in cancer treatment, theoretically. Based on those studies, we start this prospective study to investigate the effect of combination treatment of WLRT and hyperthermia on quality of life in the patients with unresectable chemoresistant liver metastasis from gastrointestinal tract cancer.
Detailed Description
1.1 gastrointestinal tract cancer liver metastasis Most mortality of the gastrointestinal tract cancer patients is related with distant metastasis, especially liver is the main site. It has been estimated that 25% of colorectal cancer patients have hepatic metastases at diagnosis, and another 50% will have their tumor recurrence in the liver within 5 years.
Selected patients who had oligo (usually 2 to 3) or isolated liver metastases resected curatively and have yielded 5-year survival rates of 50% to 60%, showing that local therapy has the potential to cure. It is only possible in less than 25% of all patients with hepatic metastasis because of medical and/or surgical reasons, furthermore two-thirds of resected patients showed ultimately liver recurrence within 2 years.
The standard treatment of unresectable liver metastasis in gastrointestinal tract cancer is chemotherapy, but considerable portion of the patients progressed and most of the liver is converted to metastatic tumor lesions. Significant quality of life decrement was detected in those patients, especially in patients suffered severe symptoms
1.2 Radiation therapy (RT) for liver metastasis Several studies reported that whole liver RT (WLRT) can be used effectively to control severe symptoms from unresectable liver metastasis in colorectal cancer patients. However, it is well known fact that the liver is a very sensitive to RT. The radiation induced liver disease (RILD), dreadful complication without special treatment method and subset of patients could be dead, can be developed as low as 30 gray (Gy). Despite symptom palliation is obtained after 20 to 30 Gy RT but only in small subset of patients get local control. In this aspect, the combined with radiosensitizer with WLRT is considered to enhance RT effect to palliate symptom and control local tumor progression, and increase the quality of life ultimately.
1.3 Hyperthermia It is reported that hyperthermia is effective in S phase, Low oxygen partial pressure (pO2), low hydrogen ion concentration (pH), and low perfusion site which are known as radio-resistant. Because of these characteristics, it considered as the most valuable radiosensitizer in cancer treatment, theoretically. Furthermore, mild hyperthermia (41 to 41.5 ºC) can promote tumor reoxygenation.
1.4 Purpose of this study Based on those studies, we start this prospective study to investigate the effect of combination treatment of WLRT and hyperthermia on quality of life in the patients with unresectable chemoresistant liver metastasis from gastrointestinal tract cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperthermia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
11 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Combined hypertermia and RT
Arm Type
Experimental
Arm Description
Combined hypertermia and radiothearpy
Intervention Type
Radiation
Intervention Name(s)
Combined hyperthermia and radiation therapy
Primary Outcome Measure Information:
Title
Time to Local Tumor Progression After Combined Hyperthermia and RT
Description
Local progression will be defined as more than 20% size increase of metastatic lesions or new metastatic lesion in liver. Time to local tumor progression will be measured from the date of RT start to the date of local progression or last follow-up visit.
Time Frame
Patient will be evaluated after combined hyperthermia and RT until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 19 months.
Secondary Outcome Measure Information:
Title
Objective Response Rate of Combined Hyperthermia and RT
Time Frame
Response will be evaluated at 3 month after combined hyperthermia and RT. Modified RECIST will be used to define resopnse.
Title
Change in the Grade of Quality of Life at 3 Months From That Before the Combined Hyperthermia and RT
Description
To measure the quality of life, European Organisation for Research and Treatment of Cancer (EORTC)- quality of life questionnaire (QLQ) 30 and Functional Assessment of Cancer Therapy-Hepatobiliary will be used. (grade 1 to 4, 1; not at all, 2; a little, 3; quite a bit, 4; very much)
Time Frame
Quality of life will be ssessed at baseline and 3 months after combined hyperthemica and RT, data reported 3 months after combined hyperthemica and RT with grade from 1 to 4.
Title
Local Tumor Progression Free Survival Rate After Combined Hyperthermia and RT
Description
Local progression will be defined as more than 20% size increase of metastatic lesions or new metastatic lesion in liver. Local progression free survival will be measured from the date of RT start to the date of local progression or last follow-up visit.
Time Frame
Response will be evaluated at 3 month after combined hyperthermia and RT. Modified RECIST will be used to define resopnse.
Title
Adverse Event After Combined Hyperthermia and RT.
Description
All grade III or higher toxicities (repeated measure)
Time Frame
Adverse event will be evaluated at 3 month. The common terminology criteria for adverse events (CTCAE) version 4.0 will be used.
Title
Overall Survival Rate After Combined Hyperthermia and RT
Description
Overall survival will be measured from the date of RT start to the date of death or last follow-up visit.
Time Frame
Pathient will be evaluated at 3 month after combined hyperthermia and RT.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1 Patients must have a diagnosis of pathologic proven gastrointestinal tract cancer
2 Unresectable and unsuitable to other local modalities
3 Not responded and/or unsuitable to chemotherapy
4 Eastern Cooperative Oncology Group ECOG) performance status 0 to 3
5 Assessment by colorectal tumor board (surgeon, radiation oncologist and medical oncologist participated)
6 Age ≥ 20
7 Agreement of study-specific informed consent
8 Blood work requirements
Absolute neutrophil count (ANC) ≥ 1,500 /mm3, Platelet ≥ 50,000/mm3, Hgb ≥ 8 g/dl
Liver function test(LFT): Total bilirubin<3.0 mg/dL, International normalized ratio(INR) < 1.7, Albumin ≥ 2.8g/dL, Aspartate aminotransferase (AST)/Alanine aminotransferase (ALT)< 6 X normal
Serum creatinine < 1.5 X normal, or Creatinine clearance rate (CCr) ≥ 60 mL/min
9 Child-Pugh score 10 or less within 1 week before WLI
10 Childbearing potential woman, consent contraception at least 6 months
11 Stable breathing more than 5 minutes
Exclusion Criteria:
1 Life expectancy less than 8 weeks
2 Pregnant and/or breastfeeding woman
3 Previous upper abdominal RT history
4 Uncontrolled ascites or hepatic encephalopathy
5 Unstable respiration due to pleural effusion, chronic obstructive pulmonary disease COPD) etc
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hee Chul Park, M.D., Ph.D.
Organizational Affiliation
Samsung Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
135-710
Country
Korea, Republic of
12. IPD Sharing Statement
Learn more about this trial
Effectiveness of the Combined WLI and Hyperthermia for GI Cancer Liver Metastasis
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